Indirect Pulp Capping With Resin Modified Glass Ionomer

Pulpitis Clinical Trial

Official title:

Indirect Pulp Capping With Resin Modified Glass Ionomer: a Randomized Controled Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02494193
• Other study ID #: IPC
• Status: Completed
• Phase: N/A
• First received: June 30, 2015
• Last updated: May 2, 2017
• Start date: June 2015
• Est. completion date: December 2016

Study information

• Verified date: May 2017
• Source: Universidade Federal de Sergipe
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In deep carious lesions, presenting risk of pulp exposition, a treatment option is the partial caries removal of carious tissue followed by provisional restoration, while this approach is called indirect pulp capping. The aim of this double-blinding controlled randomized clinical trial is to evaluate the success of indirect pulp capping using only resin-modified glass ionomer, while the additional layer of calcium hydroxide was used as control. The sample of 112 molars and/or premolars (n=56), presenting deep carious lesions, from patients with age between 15 and 30 years treated in dental clinic at Department of Dentistry of Federal University of Sergipe. The selected carious lesions must be reached 2/3 of dentin, observed in bite-wing radiography, without pulp involving and/or other factor that to compromise the evaluation. After detailed anamneses, the selected teeth will be radiographed e all carious tissue from surrounding walls will be removed. At the floor of cavity, the carious tissue will be partially removed using hand dentin excavators, remaining the caries-affected dentin and avoiding the pulp exposition. The removed carious tissue from the floor of cavity will be evaluated for presence of Lactobacilos e Estreptococos Mutans, while the remaining dentin will be evaluated for consistency, colour and humidity. Randomly, the cavity will be provisionally restored with: Control - dress and cement of calcium hydroxide followed resin-modified glass ionomer; or Experimental - only resin-modified glass ionomer. The distance between the base of restoration and the pulp cavity cap will be measured by bitw-wing radiography. The patients will be re-evaluated after 15 days, while the teeth with compromised pulp vitality will be excluded from the study. The remaining patients will be evaluated after 6 months. The distance between the base of restoration and the pulp cavity cap will be measured again, followed by provisional restoration removal. The remaining caries-affected dentin from floor of cavity will be fully removed and a bacteriological evaluation performed. The consistency, colour and humidity of this tissue will be evaluated too. Finally, the permanent restorations will performed.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 112
• Est. completion date: December 2016
• Est. primary completion date: September 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 15 Years to 30 Years

Eligibility

Inclusion Criteria:

• Molars and pre-molars presenting carious lesions involving 2/3 inner of dentin tissue.

Exclusion Criteria:

• Teeth presenting signs of irreversible pulpits or necrose, cervical lesion and/or root exposition, or with carious lesion reaching the pulp.

Related Conditions & MeSH terms

• Caries, Dental
• Dental Caries
• Pulpitis

Intervention

Other:
• Partial caries removal
The caries infected dentin will be removed mantaining the affected caries tissue.
• Provisional restoration - control
After partial caries removal, a provisional restoration will be performed using a layer of calcium hydroxide paste covered by a layer of calcium hydroxide cement and resin-modified glass ionomer.
• Provisional restoration - experimental
After partial caries removal, a provisional restoration will be performed using only resin-modified glass ionomer.
• Total caries removal
After two months of their placement, the provisional restoration will removed followed by tota caries tissue removal.
• Definitive restoration
Definite restoration will be performed using composite.

Locations

Country	Name	City	State
Brazil	Universidade Federal de Sergipe	Aracaju	SE

Sponsors (1)

Lead Sponsor	Collaborator
Universidade Federal de Sergipe

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Tooth vitality - analysis for positive or negative response		2 months after placement of provisional restoration
Secondary	Consistency of dentin tissue - scores of 1 (softned) to 4 (hard)		Immediately after caries removal
Secondary	Coloration of dentin tissue - scores of 1 (clear yellow) to 5 (darkd)		Immediately after caries removal
Secondary	Counting of Streptococcus mutans colonies - number of colony-forming units (CFUs)		Immediately after caries removal
Secondary	Counting of Lactobacillus spp colonies - number of colony-forming units (CFUs)		Immediately after caries removal